Tumor Treating Fields (TTFields) therapy after stereotactic radiosurgery for brain metastases from non-small cell lung cancer: final results of the phase 3 METIS study.

IF 6.5 1区 医学 Q1 ONCOLOGY
Minesh P Mehta, Vinai Gondi, Manmeet Singh Ahluwalia, David Roberge, Terence Tai Weng Sio, Daniel M Trifiletti, Thierry Muanza, Ana Misir Krpan, Zhengfei Zhu, Naren R Ramakrishna, John B Fiveash, Philippe Metellus, Jinming Yu, Chiachien Jake Wang, Julian Jacob, Christian F Freyschlag, Tibor Csőszi, Andrea Salmaggi, Alisa Taliansky, Ana Lucas, Jürgen Debus, Paul D Brown, Maciej Harat
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引用次数: 0

Abstract

Purpose: Improved treatments for brain metastases from non-small cell lung cancer (NSCLC BM) are needed to prolong time to intracranial progression without increasing neurotoxicity. TTFields, are electric fields delivered via skin-based arrays that disrupt cancer cell division, have demonstrated efficacy and safety in glioblastoma, NSCLC, and pancreatic cancer.

Methods and materials: In the phase 3 METIS trial (NCT02831959) adults with 1-10 newly-diagnosed NSCLC BM suitable for SRS receiving optimal therapy for extracranial disease were randomized 1:1 to SRS followed by TTFields (150 kHz) or SRS alone. Radiologic progression was assessed by an independent radiology review committee. Primary endpoint was time to intracranial progression (TTIP; RANO-BM). Secondary endpoints included overall survival, neurocognitive function, quality of life (QoL), and safety.

Results: Patients (N=298) were followed for a median of 8.6 (0.07-85.2) months. TTFields significantly delayed TTIP (HR 0.72 [95% CI 0.53-0.98]; Fine-Gray P=0.044). Intracranial progression rates at months 2, 6, 12, and 24 were 13.6% vs 22.1% (P=0.034), 33.7% vs 46.4% (P=0.018), 46.9% vs 59.4% (P=0.023), and 53.6% vs 65.2% (P=0.031; post hoc). Time to distant intracranial progression (TTDP) favored TTFields therapy, although not statistically significantly (HR 0.76 [0.51-1.12]; log-rank P=0.165; post-hoc). In patients receiving immune checkpoint inhibitors (ICI; n=118), the delays in both TTIP (HR 0.63 [0.39-1.0]; Cox P=0.049; Fine-Gray P=0.055) and TTDP (HR 0.41 [0.21-0.81]; log-rank P=0.0087, post-hoc) were more pronounced. Device-related AEs were mainly grade ≤2 skin events. TTFields did not cause QoL deterioration, and improvements in deterioration-free survival and time to deterioration of the global health status, physical functioning and fatigue domains were observed (post-hoc).

Conclusions: By significantly prolonging TTIP, without worsening QoL or cognitive function, TTFields after SRS is a new treatment option for patients with NSCLC BM, including those receiving ICI.

非小细胞肺癌脑转移的立体定向放射手术后肿瘤治疗场(TTFields)治疗:3期METIS研究的最终结果
目的:非小细胞肺癌(NSCLC)脑转移瘤需要改进治疗,以延长颅内进展时间而不增加神经毒性。TTFields是一种通过皮肤阵列传递的电场,可破坏癌细胞分裂,已被证明在胶质母细胞瘤、非小细胞肺癌和胰腺癌中具有有效性和安全性。方法和材料:在3期METIS试验(NCT02831959)中,1-10例新诊断的适合SRS的NSCLC BM接受最佳颅外疾病治疗的成年人被1:1随机分配到SRS,然后是TTFields (150 kHz)或单独SRS。放射学进展由独立的放射学审查委员会评估。主要终点是颅内进展时间(TTIP; RANO-BM)。次要终点包括总生存期、神经认知功能、生活质量(QoL)和安全性。结果:298例患者的随访时间中位数为8.6(0.07-85.2)个月。TTFields显著延迟TTIP (HR 0.72 [95% CI 0.53-0.98]; Fine-Gray P=0.044)。颅内进展率在第2、6、12和24个月分别为13.6% vs 22.1% (P=0.034)、33.7% vs 46.4% (P=0.018)、46.9% vs 59.4% (P=0.023)和53.6% vs 65.2% (P=0.031)。远端颅内进展时间(TTDP)有利于TTFields治疗,尽管没有统计学意义(HR 0.76 [0.51-1.12]; log-rank P=0.165; post-hoc)。在接受免疫检查点抑制剂(ICI, n=118)的患者中,TTIP (HR 0.63 [0.39-1.0]; Cox P=0.049; Fine-Gray P=0.055)和TTDP (HR 0.41 [0.21-0.81]; log-rank P=0.0087,事后)的延迟更为明显。器械相关ae主要为≤2级皮肤事件。TTFields不会导致生活质量恶化,并且观察到无恶化生存期和总体健康状况、身体功能和疲劳域恶化时间的改善(事后)。结论:通过显著延长TTIP,不恶化生活质量或认知功能,TTFields在SRS后是NSCLC BM患者的一种新的治疗选择,包括那些接受ICI的患者。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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